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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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STRUMENTARIO CHIRURGICO — 4 UDI-DI variants, MDR (Silfradent S.R.L.)

MD Atlas
Silfradent S.R.L.

Data from EUDAMED, last updated May 31, 2026

STRUMENTARIO CHIRURGICO

805609331STCHG6

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Silfradent S.R.L.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 805609331STCHG6
Device name: STRUMENTARIO CHIRURGICO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: Silfradent S.R.L.
SRN: IT-MF-000018668
Country: Italy
Email: info@silfradent.com
Phone: +39 0543 970684

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KK9H5ZJK20F4E3HM0TPM5E09

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

RU200CI08056093310771
CGF K1 - FMP08056093310757
CGF K1 - GSP08056093310740
CGF K1 - TRA08056093310764